Canonical Allele Identifier: CA2661822913
Gene: LRP2 HGNC NCBI

Linked Data

gnomAD v4: 2-169259245-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.169259245A>T , CM000664.2:g.169259245A>T GRCh38
NC_000002.11:g.170115755A>T , CM000664.1:g.170115755A>T GRCh37
NC_000002.10:g.169824001A>T NCBI36
NG_012634.1:g.108368T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000649046.1:c.2321-28T>A MANE Select ENSP00000496870.1:n.2321-28T>A
ENST00000263816.7:c.2321-28T>A ENSP00000263816.3:n.2321-28T>A
ENST00000443831.1:c.1910-28T>A ENSP00000409813.1:n.1910-28T>A
NM_004525.2:c.2321-28T>A NP_004516.2:n.2321-28T>A
XM_011511183.1:c.2321-28T>A XP_011509485.1:n.2321-28T>A
XM_011511184.1:c.32-28T>A XP_011509486.1:n.32-28T>A
XM_011511185.1:c.2321-28T>A XP_011509487.1:n.2321-28T>A
NM_004525.3:c.2321-28T>A MANE Select NP_004516.2:n.2321-28T>A
XM_011511183.3:c.2321-28T>A XP_011509485.1:n.2321-28T>A
XM_011511184.2:c.32-28T>A XP_011509486.1:n.32-28T>A
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